37876
Anilofos
PESTANAL®, analytical standard
Synonym(s):
S-[2-(4-Chloro-N-isopropylanilino)-2-oxoethyl]-O,O′-dimethyl dithiophosphate
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About This Item
Empirical Formula (Hill Notation):
C13H19ClNO3PS2
CAS Number:
Molecular Weight:
367.85
Beilstein:
2395778
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
Recommended Products
grade
analytical standard
Quality Level
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
storage temp.
2-8°C
SMILES string
COP(=S)(OC)SCC(=O)N(C(C)C)c1ccc(Cl)cc1
InChI
1S/C13H19ClNO3PS2/c1-10(2)15(12-7-5-11(14)6-8-12)13(16)9-21-19(20,17-3)18-4/h5-8,10H,9H2,1-4H3
InChI key
NXQDBZGWYSEGFL-UHFFFAOYSA-N
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General description
Anilofos is a pre-emergence, organophosphorus herbicide, which is commonly used for the control of various annual grass weeds and sedges such as barnyard grasses in rice-based cropping system. Its mode of action involves the inhibition of cell division stage in weeds.
Application
Anilofos may be used as an analytical reference standard for the quantification of the analyte in environmental samples using stir bar sorptive extraction and thermal desorption combined with gas chromatography coupled to mass spectrometry.
Anilofos may be used as an analytical reference standard for the quantification of the analyte in environmental samples using stir bar-sorptive extraction and thermal desorption combined with gas chromatography coupled to mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Recommended products
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
>212.0 °F - closed cup
Flash Point(C)
> 100 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Bioefficacy and determination of terminal residues of a herbicide anilofos in field soil and plants following an application to the transplanted rice crop
Sondhia S and Dixit A
Communications in Soil Science and Plant Analysis, 46(20), 2576-2584 (2015)
Dilek Akyil et al.
Cytotechnology, 69(6), 865-874 (2017-06-14)
We aimed to evaluate the mutagenic effect of Anilofos, organophosphate pesticide, by using Ames/Salmonella/microsome test. Its cytotoxic and genotoxic effects were also determined by chromosome aberration (CA), sister chromatid exchange (SCE) and micronucleus (MN) test in human peripheral blood lymphocytes.
Simultaneous determination of 64 pesticides in river water by stir bar sorptive extraction and thermal desorption-gas chromatography-mass spectrometry
Nakamura S and Daishima S
Analytical and Bioanalytical Chemistry, 382(1), 99-107 (2005)
Jishi Wang et al.
Journal of chromatography. A, 1521, 10-18 (2017-09-25)
In this research, the manual two-step QuEChERS approach has been streamlined and automated into a one-step method using a cleanup tube fitted within an extraction tube. A novel automatic QuEChERS combination have been developed to simplify the QuEChERS procedures and
Jaswant Singh et al.
Food chemistry, 327, 127080-127080 (2020-05-27)
A hydrazone based Schiff base (SB) has been synthesized and investigated for the detection, quantification and degradation of selective organophosphates (i.e diethyl chlorophosphate, diethyl cyanophosphonate, tris (2-chloroethyl) phosphate and dichlorvos). The organophosphates (OPs) form a covalent bond with -OH groups
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